Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2064478
rs2064478
2 0.925 0.200 6 33104489 intron variant C/T snv 0.28 0.700 1.000 2 2007 2009
dbSNP: rs2064476
rs2064476
2 0.925 0.200 6 33105545 intron variant A/G snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs3117231
rs3117231
1 1.000 0.120 6 33107131 intron variant A/G snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs3128927
rs3128927
1 1.000 0.120 6 33106511 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs3130215
rs3130215
3 0.882 0.240 6 33107186 intron variant A/G snv 0.69 0.700 1.000 1 2007 2007